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A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease
BACKGROUND: The aim of this study was to explore the clinical relevance of linear measures of Wilson's disease (WD). METHODS: Relative values of brain atrophy in 30 patients with WD and 30 healthy volunteers were measured and compared using a manual measurement method. Linear measurement indica...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086176/ https://www.ncbi.nlm.nih.gov/pubmed/37056963 http://dx.doi.org/10.3389/fnhum.2023.1142082 |
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author | Wang, Yun Xuan, Hongxia Zhao, Tun Li, Xiaodong Li, Shujuan Hu, Wenli |
author_facet | Wang, Yun Xuan, Hongxia Zhao, Tun Li, Xiaodong Li, Shujuan Hu, Wenli |
author_sort | Wang, Yun |
collection | PubMed |
description | BACKGROUND: The aim of this study was to explore the clinical relevance of linear measures of Wilson's disease (WD). METHODS: Relative values of brain atrophy in 30 patients with WD and 30 healthy volunteers were measured and compared using a manual measurement method. Linear measurement indicators of brain atrophy in patients with and without mental disorders were also compared. In addition, correlations of patients' age, disease duration, and Unified Wilson's Disease Rating Scale (UWDRS) scores with brain atrophy indicators were determined. RESULTS: The results showed that the e-value, Huckman number, Evans index, and lateral ventricular body index were higher in the WD group compared with the control group. The age of patients with WD was negatively correlated with the k-value and significantly positively correlated with the brainstem index. WD duration was prominently positively correlated with the d-value and negatively correlated with the j-value. In addition, neurological function scores were significantly positively correlated with the c-value, e-value, caudate nucleus index, Huckman number, Evans index, and lateral ventricular body index. By contrast, patients with psychiatric symptoms had a higher a-value and fourth ventricular index than those without psychiatric symptoms. CONCLUSION: Therefore, it can be concluded that patients with WD and those with psychiatric symptoms have more severe brain atrophy compared to normal subjects. The patient's age, disease duration, and neurological function scores were positively correlated with the severity of brain atrophy. |
format | Online Article Text |
id | pubmed-10086176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100861762023-04-12 A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease Wang, Yun Xuan, Hongxia Zhao, Tun Li, Xiaodong Li, Shujuan Hu, Wenli Front Hum Neurosci Human Neuroscience BACKGROUND: The aim of this study was to explore the clinical relevance of linear measures of Wilson's disease (WD). METHODS: Relative values of brain atrophy in 30 patients with WD and 30 healthy volunteers were measured and compared using a manual measurement method. Linear measurement indicators of brain atrophy in patients with and without mental disorders were also compared. In addition, correlations of patients' age, disease duration, and Unified Wilson's Disease Rating Scale (UWDRS) scores with brain atrophy indicators were determined. RESULTS: The results showed that the e-value, Huckman number, Evans index, and lateral ventricular body index were higher in the WD group compared with the control group. The age of patients with WD was negatively correlated with the k-value and significantly positively correlated with the brainstem index. WD duration was prominently positively correlated with the d-value and negatively correlated with the j-value. In addition, neurological function scores were significantly positively correlated with the c-value, e-value, caudate nucleus index, Huckman number, Evans index, and lateral ventricular body index. By contrast, patients with psychiatric symptoms had a higher a-value and fourth ventricular index than those without psychiatric symptoms. CONCLUSION: Therefore, it can be concluded that patients with WD and those with psychiatric symptoms have more severe brain atrophy compared to normal subjects. The patient's age, disease duration, and neurological function scores were positively correlated with the severity of brain atrophy. Frontiers Media S.A. 2023-03-28 /pmc/articles/PMC10086176/ /pubmed/37056963 http://dx.doi.org/10.3389/fnhum.2023.1142082 Text en Copyright © 2023 Wang, Xuan, Zhao, Li, Li and Hu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Human Neuroscience Wang, Yun Xuan, Hongxia Zhao, Tun Li, Xiaodong Li, Shujuan Hu, Wenli A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease |
title | A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease |
title_full | A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease |
title_fullStr | A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease |
title_full_unstemmed | A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease |
title_short | A study of linear measurement and clinical correlation of brain atrophy in Wilson's disease |
title_sort | study of linear measurement and clinical correlation of brain atrophy in wilson's disease |
topic | Human Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086176/ https://www.ncbi.nlm.nih.gov/pubmed/37056963 http://dx.doi.org/10.3389/fnhum.2023.1142082 |
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